rs8099917, None

N. diseases: 60
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Chronic hepatitis C virus genotype 1
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2014
Acute hepatitis C
CUI: C0400914
Disease: Acute hepatitis C
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
Congenital Bleeding Disorder
CUI: C3641106
Disease: Congenital Bleeding Disorder
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Hepatitis D, Chronic
CUI: C0524911
Disease: Hepatitis D, Chronic
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Chronic hepatitis C genotype 4
CUI: C4049431
Disease: Chronic hepatitis C genotype 4
3 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Hepatitis D Infection
CUI: C0011226
Disease: Hepatitis D Infection
4 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Infectious Mononucleosis
CUI: C0021345
Disease: Infectious Mononucleosis
4 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Tropical Spastic Paraparesis
CUI: C0030481
Disease: Tropical Spastic Paraparesis
4 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Mixed cryoglobulinemia
CUI: C0543697
Disease: Mixed cryoglobulinemia
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.030 1.000 3 2013 2017
Recurrent hepatitis
CUI: C3887641
Disease: Recurrent hepatitis
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2014
Acute infectious disease
CUI: C0275518
Disease: Acute infectious disease
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
HTLV-I Infections
CUI: C0020097
Disease: HTLV-I Infections
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Subacute Sclerosing Panencephalitis
CUI: C0038522
Disease: Subacute Sclerosing Panencephalitis
6 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2018 2018
Cryoglobulinemia
CUI: C0010403
Disease: Cryoglobulinemia
7 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2015 2015
Hemophilia, NOS
CUI: C0684275
Disease: Hemophilia, NOS
8 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
Arthropathy
CUI: C0022408
Disease: Arthropathy
10 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2016 2016
Congenital hypoplasia of adrenal gland
13 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
TROPICAL CALCIFIC PANCREATITIS
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
13 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Kaposi Sarcoma
CUI: C0036220
Disease: Kaposi Sarcoma
15 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2018 2018
Sensory neuropathy
CUI: C0151313
Disease: Sensory neuropathy
15 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
Icterus
CUI: C0022346
Disease: Icterus
17 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2010 2019
Influenza
CUI: C0021400
Disease: Influenza
17 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Thalassemia
CUI: C0039730
Disease: Thalassemia
18 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Cooley's anemia
CUI: C0002875
Disease: Cooley's anemia
19 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Severe Dengue
CUI: C0019100
Disease: Severe Dengue
25 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1 2018 2018